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The ionization potentials of these compounds range from 5.45 to 5.97 as determined by the electron photoemission method.
The compounds range from C6 to >C33, including n-alkanols, n-alkanoic acids, n-alkyl formates, n-alkanones, and n-alkanes, all with no carbon number preferences.
Compounds range from potent ligands (Ki = 1 nM) to potent inhibitors (14 nM), and include one compound [NMDPEF: N-[2- 2-methoxy-6H-dipyrido[2,3-a 3,2-e]pyrrolizin-11-yl)ethyl]-2-furamide] active oN-[2- 2-methoxy-6H-dipyrido[2,3-a 3,2-e]pyrrolizin-11-yl
IC50 values of these compounds range from 2 nM to 150 nM.
Neptunium VI) compounds range from the simple oxalate (which is unstable, usually becoming Np(IV)) to such complicated compounds as the green.
The approaches for selecting plants to be tested for new bioactive compounds range from random selection to ethnopharmalogical approaches relying on knowledge gained from traditional medicine usage.
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Lag-times for the start of degradation of these compounds ranged from < 15 to 30 days.
The binding affinity of the new compounds ranged from 6 to 133 nM.
The MIC value of these compounds ranged from 1.56 μg/mL to 100 μg/mL.
Next, proliferation of Tg and Nc was tested in the presence of a concentration series of these compounds ranging from 0 to 20 nM.
Evaluation in the reporter-gene assay showed that the compounds ranged from non-active to compounds more potent than 1.
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